Canonical Allele Identifier: CA477582276

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750578G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880683G>A , CM000673.2:g.130880683G>A	GRCh38
NC_000011.9:g.130750578G>A , CM000673.1:g.130750578G>A	GRCh37
NC_000011.8:g.130255788G>A	NCBI36
NG_053190.1:g.40806C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2697C>T MANE Select	ENSP00000265909.4:p.Thr899=
ENST00000265909.8:c.2697C>T	ENSP00000265909.4:p.Thr899=
ENST00000426933.6:c.201C>T	ENSP00000413345.2:p.Thr67=
ENST00000526579.5:n.178-972C>T
ENST00000527116.5:n.459C>T
ENST00000528555.5:c.837C>T	ENSP00000435122.1:p.Thr279=
ENST00000530330.1:n.433C>T
ENST00000530356.5:c.837C>T	ENSP00000432307.1:p.Thr279=
ENST00000533318.5:n.1057C>T
ENST00000534726.5:c.417C>T	ENSP00000433699.1:p.Thr139=
NM_001301089.1:c.837C>T	NP_001288018.1:p.Thr279=
NM_014758.2:c.2697C>T	NP_055573.2:p.Thr899=
XM_005271546.3:c.2574-972C>T	XP_005271603.1:n.2574-972C>T
XM_011542819.1:c.2943C>T	XP_011541121.1:p.Thr981=
XM_011542820.1:c.2931C>T	XP_011541122.1:p.Thr977=
XM_011542821.1:c.2823C>T	XP_011541123.1:p.Thr941=
XM_011542824.1:c.2061C>T	XP_011541126.1:p.Thr687=
XM_011542825.1:c.1218C>T	XP_011541127.1:p.Thr406=
XM_011542826.1:c.1083C>T	XP_011541128.1:p.Thr361=
XM_011542827.1:c.963C>T	XP_011541129.1:p.Thr321=
NM_001347918.1:c.2577C>T	NP_001334847.1:p.Thr859=
NM_001347919.1:c.2574-972C>T	NP_001334848.1:n.2574-972C>T
NM_001347922.1:c.1026C>T	NP_001334851.1:p.Thr342=
NM_001347923.1:c.972C>T	NP_001334852.1:p.Thr324=
NM_001347924.1:c.717C>T	NP_001334853.1:p.Thr239=
NM_001347925.1:c.663C>T	NP_001334854.1:p.Thr221=
NM_001347926.1:c.714-972C>T	NP_001334855.1:n.714-972C>T
NM_001347927.1:c.417C>T	NP_001334856.1:p.Thr139=
NR_144939.1:n.3330C>T
XM_011542820.2:c.2931C>T	XP_011541122.1:p.Thr977=
XM_011542821.3:c.2823C>T	XP_011541123.1:p.Thr941=
XM_011542824.2:c.2061C>T	XP_011541126.1:p.Thr687=
XM_011542825.2:c.1218C>T	XP_011541127.1:p.Thr406=
XM_011542826.2:c.1083C>T	XP_011541128.1:p.Thr361=
XM_024448521.1:c.2943C>T	XP_024304289.1:p.Thr981=
XR_001747870.1:n.3768C>T
XR_001747872.1:n.3114C>T
XR_001747873.1:n.3428C>T
NM_001301089.2:c.837C>T	NP_001288018.1:p.Thr279=
NM_001347918.2:c.2577C>T	NP_001334847.2:p.Thr859=
NM_001347919.2:c.2574-972C>T	NP_001334848.2:n.2574-972C>T
NM_001347920.2:c.*21093C>T	NP_001334849.2:n.*21093C>T
NM_001347922.2:c.1026C>T	NP_001334851.2:p.Thr342=
NM_001347923.2:c.972C>T	NP_001334852.2:p.Thr324=
NM_001347924.2:c.717C>T	NP_001334853.1:p.Thr239=
NM_001347925.2:c.663C>T	NP_001334854.1:p.Thr221=
NM_001347926.2:c.714-972C>T	NP_001334855.1:n.714-972C>T
NM_001347927.2:c.417C>T	NP_001334856.1:p.Thr139=
NM_014758.3:c.2697C>T MANE Select	NP_055573.3:p.Thr899=
NR_144939.2:n.3322C>T